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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367495Generated: October 30, 2026

Sodium borohydride → tert-Butyl 3-hydroxycyclopentanecarboxylate

https://huagongshe.com/reaction/1367495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl 3-oxocyclopentane-1-carboxylateHCID 14009986—
SolventMethanolHCID 887—
Producttert-Butyl 3-hydroxycyclopentanecarboxylateHCID 1400998867%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a cold (ice bath) solution of Rac-3-Oxo-cyclopentanecarboxylic acid tert-butyl ester (1.43 g) in methanol (9 mL) was added sodium borohydride (0.293 g). The mixture was stirred 25 min at 0-5° C. then concentrated in vacuo. Ethyl acetate was added to the residue and the mixture was washed with water, dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography on silica gel with dichloromethane/methanol (19:1 v/v) as eluant to afford the title compound (0.963 g, 67%) as colorless oil. MS (EI): 187.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893099B2
Source datasetuspto-grants-2011_02
ORD IDord-725cfe38759e40028e982469be08d622
Source noteuspto-grants-2011_02